Hancock™ HC150-20Recalls & reported problems
Medtronic, Inc. · CONDUIT HC150-20 HK1 MO 26L · Class 3 · Implant
All models of HANCOCK (22)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000517823), received between Nov 1, 2024 and Nov 1, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Packaging Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Packaging Problem1
- Unsealed Device Packaging1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 1, 2024Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF THIS 20MM PULMONARY VALVED CONDUIT, IT WAS REPORTED THAT THE GLASS STORAGE TUBE CONTAINING THE CONDUIT WAS OBSERVED TO HAVE CRACKED AND ALL FLUIDS DRAINED UPON OPENING THE BOX. IT WAS NOTED THAT A PORTION OF THE GLASS STORAGE TUBE HAD BROKEN OFF. IT WAS STATED THAT THE SURROUNDING AREA WHERE THE BOX WAS KEPT SHOWED NO SIGNS OF WETNESS. IT WAS ALSO STATED THAT THERE WERE NO SIGNS OF PACKAGING WETNESS OR DAMAGE AND DAMAGE WAS ONLY DISCOVERED UPON OPENING THE PACKAGE. NO PATIENT INVOLVEMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20585600 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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